Inoue Keita, Kato Harunosuke, Sato Takahiro, Osada Aki, Aoi Noriyuki, Suga Hirotaka, Eto Hitomi, Gonda Koichi, Yoshimura Kotaro
Department of Plastic Surgery, University of Tokyo School of Medicine, Tokyo, Japan.
Cells Tissues Organs. 2009;190(2):102-10. doi: 10.1159/000178021. Epub 2008 Nov 26.
The dermal papilla (DP) interacts with epithelial cells for folliculogenesis. For translational research on cell therapies for hair regrowth with cultured human DP cells (hDPCs), a model to evaluate the capacity of hDPCs to induce hair formation is inevitable.
Chamber models were constructed by transplanting 4 different combinations of mouse or human epithelial and mesenchymal cells into a silicone chamber implanted onto the back of nude mice. In parallel, 3 types of sandwich constructs were created by inserting hDPCs or human DP tissue between the epidermis and dermis of isolated rat footpad skin or human facial skin, and subcutaneously transplanting the constructs into the back of nude mice. Four to six weeks later, skin sections of each model were histologically examined.
Folliculoneogenesis was detected in both chamber and sandwich models, although the induction rate and maturity of the hair follicles varied among cell combination subgroups in each model. The difference in hair induction rate was not statistically significant between 2 representative chamber and sandwich subgroups using cultured hDPCs. The sandwich model, however, required fewer hDPCs, did not require human keratinocytes, and exhibited a higher rate of successful sample collection.
Although there is no significant difference in hair induction rate, the sandwich model using cultured hDPCs and the rat sole skin is more feasible than the chamber model using human cultured keratinocytes and hDPCs as a tool to evaluate the hair-inducing capacity of cultured hDPCs.
真皮乳头(DP)与上皮细胞相互作用以促进毛囊形成。对于利用培养的人真皮乳头细胞(hDPCs)进行毛发再生细胞治疗的转化研究,建立一个评估hDPCs诱导毛发形成能力的模型是必不可少的。
通过将4种不同组合的小鼠或人上皮细胞和间充质细胞移植到植入裸鼠背部的硅胶室中构建室模型。同时,通过将hDPCs或人DP组织插入分离的大鼠足垫皮肤或人面部皮肤的表皮和真皮之间,并将构建体皮下移植到裸鼠背部,创建3种类型的三明治构建体。4至6周后,对每个模型的皮肤切片进行组织学检查。
在室模型和三明治模型中均检测到毛囊新生,尽管每个模型中细胞组合亚组之间毛囊的诱导率和成熟度有所不同。使用培养的hDPCs的2个代表性室模型和三明治模型亚组之间的毛发诱导率差异无统计学意义。然而,三明治模型所需的hDPCs较少,不需要人角质形成细胞,并且样本采集成功率较高。
尽管毛发诱导率没有显著差异,但使用培养的hDPCs和大鼠足底皮肤的三明治模型作为评估培养的hDPCs毛发诱导能力的工具比使用人培养角质形成细胞和hDPCs的室模型更可行。